Cargando…

The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine

Human cytomegalovirus (HCMV) infection is a major cause of morbidity in the recipients of organ transplants and in the congenitally infected infants. HCMV vaccine has emerged as an effective approach to prevent HCMV infection particularly for the development of multiple viral antigens vaccination an...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ping, Ma, Dao-Xin, Yu, Shuang, Xue, Fu-Zhong, Zhu, Wei-Wei, Shao, Na, Zhang, Jing-Ru, Ji, Chun-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114286/
https://www.ncbi.nlm.nih.gov/pubmed/22197248
http://dx.doi.org/10.1016/j.antiviral.2011.12.005
_version_ 1783513852756885504
author Zhao, Ping
Ma, Dao-Xin
Yu, Shuang
Xue, Fu-Zhong
Zhu, Wei-Wei
Shao, Na
Zhang, Jing-Ru
Ji, Chun-Yan
author_facet Zhao, Ping
Ma, Dao-Xin
Yu, Shuang
Xue, Fu-Zhong
Zhu, Wei-Wei
Shao, Na
Zhang, Jing-Ru
Ji, Chun-Yan
author_sort Zhao, Ping
collection PubMed
description Human cytomegalovirus (HCMV) infection is a major cause of morbidity in the recipients of organ transplants and in the congenitally infected infants. HCMV vaccine has emerged as an effective approach to prevent HCMV infection particularly for the development of multiple viral antigens vaccination and human leukocyte antigen (HLA)-restricted polyepitope technology. As the Chinese population makes up more than one fifth of the population worldwide, it is important to develop HCMV vaccines more specific for the Chinese population by targeting Chinese-restricted HLA alleles and antigens. In the present study, we designed a novel chimeric polyepitope vaccine based on the replication-deficient adenovirus Ad5F35, which encodes 83 HCMV T cell epitopes from 15 different HCMV antigens, restricted to 14 HLA I and 7 HLA II alleles that cover 92% of the Chinese population. Our results show that the recombinant adenovirus vaccine Ad5F35-CTL·Th can be efficiently transfected and expressed in peripheral blood mononuclear cells (PBMCs) with little cytopathic activity. Ad5F35-CTL·Th can also be endogenously processed and presented by PBMCs. Ad5F35-CTL·Th-stimulated HCMV-specific cytotoxic T lymphocytes (CTLs) showed strong cytolytic activity against HCMV polyepitope-sensitized target cells. The CTL activity was accompanied by high levels of IFN-γ production after Ad5F35-CTL·Th stimulation. The specificity and vigorous response to the recombinant adenovirus vaccine in vitro makes it a potential candidate to be used for transplantation recipients or congenitally infected infants.
format Online
Article
Text
id pubmed-7114286
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-71142862020-04-02 The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine Zhao, Ping Ma, Dao-Xin Yu, Shuang Xue, Fu-Zhong Zhu, Wei-Wei Shao, Na Zhang, Jing-Ru Ji, Chun-Yan Antiviral Res Article Human cytomegalovirus (HCMV) infection is a major cause of morbidity in the recipients of organ transplants and in the congenitally infected infants. HCMV vaccine has emerged as an effective approach to prevent HCMV infection particularly for the development of multiple viral antigens vaccination and human leukocyte antigen (HLA)-restricted polyepitope technology. As the Chinese population makes up more than one fifth of the population worldwide, it is important to develop HCMV vaccines more specific for the Chinese population by targeting Chinese-restricted HLA alleles and antigens. In the present study, we designed a novel chimeric polyepitope vaccine based on the replication-deficient adenovirus Ad5F35, which encodes 83 HCMV T cell epitopes from 15 different HCMV antigens, restricted to 14 HLA I and 7 HLA II alleles that cover 92% of the Chinese population. Our results show that the recombinant adenovirus vaccine Ad5F35-CTL·Th can be efficiently transfected and expressed in peripheral blood mononuclear cells (PBMCs) with little cytopathic activity. Ad5F35-CTL·Th can also be endogenously processed and presented by PBMCs. Ad5F35-CTL·Th-stimulated HCMV-specific cytotoxic T lymphocytes (CTLs) showed strong cytolytic activity against HCMV polyepitope-sensitized target cells. The CTL activity was accompanied by high levels of IFN-γ production after Ad5F35-CTL·Th stimulation. The specificity and vigorous response to the recombinant adenovirus vaccine in vitro makes it a potential candidate to be used for transplantation recipients or congenitally infected infants. Elsevier B.V. 2012-02 2011-12-13 /pmc/articles/PMC7114286/ /pubmed/22197248 http://dx.doi.org/10.1016/j.antiviral.2011.12.005 Text en Copyright © 2011 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Zhao, Ping
Ma, Dao-Xin
Yu, Shuang
Xue, Fu-Zhong
Zhu, Wei-Wei
Shao, Na
Zhang, Jing-Ru
Ji, Chun-Yan
The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title_full The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title_fullStr The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title_full_unstemmed The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title_short The development of Chinese specific human cytomegalovirus polyepitope recombinant vaccine
title_sort development of chinese specific human cytomegalovirus polyepitope recombinant vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114286/
https://www.ncbi.nlm.nih.gov/pubmed/22197248
http://dx.doi.org/10.1016/j.antiviral.2011.12.005
work_keys_str_mv AT zhaoping thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT madaoxin thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT yushuang thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT xuefuzhong thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT zhuweiwei thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT shaona thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT zhangjingru thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT jichunyan thedevelopmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT zhaoping developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT madaoxin developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT yushuang developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT xuefuzhong developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT zhuweiwei developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT shaona developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT zhangjingru developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine
AT jichunyan developmentofchinesespecifichumancytomegaloviruspolyepitoperecombinantvaccine